Canonical Allele Identifier: PA106511
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2666
ClinVar RCV Id: RCV000002785 RCV001582462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_877437.2:p.Arg349Trp
CA115671
NM_182760.4:c.1045C>T